chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	59153550	59153551	C	T	48	GENIC	homozygous	111582774
3	59153622	59153623	T	C	52	GENIC	homozygous	111582775
3	59153632	59153633	G	C	50	GENIC	homozygous	111582776
3	59153812	59153813	A	G	58	GENIC	homozygous	111582777
3	59154184	59154185	C	G	41	GENIC	homozygous	111582778
3	59154243	59154243		TTGGGC	39	GENIC	homozygous	127887104
3	59154952	59154953	T	G	39	GENIC	homozygous	111582779
3	59155052	59155052		CAAAGA	51	GENIC	homozygous	127887105
3	59155054	59155054		TA	49	GENIC	homozygous	127887106
3	59155172	59155173	G	A	51	GENIC	homozygous	111582780
3	59155211	59155212	T	A	50	GENIC	homozygous	111582781
3	59155655	59155656	A	G	57	GENIC	homozygous	111582782
3	59155853	59155858	TTTAA		33	GENIC	heterozygous	127887107
3	59156158	59156159	A	C	65	GENIC	homozygous	111582783
3	59156233	59156233		AA	46	GENIC	homozygous	127887108
3	59156666	59156667	T	A	52	GENIC	homozygous	111582784
3	59156930	59156931	C		31	GENIC	homozygous	127887109
3	59160301	59160302	A	G	60	GENIC	homozygous	111582785
3	59161102	59161103	A	G	62	GENIC	homozygous	111582786
3	59162534	59162535	C	T	56	GENIC	homozygous	111582787